Ah I love your travel vlogs! It's always so nice to see what you're getting up to and all the accessibility of these destinations. It's lovely to see and fun to daydream about 😊

You're a really good travel vlogger! You're funny, the places you visit are interesting and all the tips you have for people with disabilities and dietary restrictions are pure gold! I like how you do the tips last, it's a format that has a good flow. Thanks for everything that you share with us! 🙏❤ Side note: I highly recommended the 2008 comedy, "In Bruges," for those who haven't seen it, it shows the beauty of Bruges and is hilarious!

Hi what is the disabled bathroom in your hotel like? I know what it is like to zipping with a wheelchair you do need 2 people because you do need to take the wheelchair away

Aw Pippa, Bruges looks stunning. I love watching your travel vlogs and am excited to see where your next few trips will be.

i'm staying in the exact same london hotel for my eurostar journey next month 😂 i'm really nervous (only been abroad once when i was young) but this is such a helpful video Pippa!!

You can watch the vlog from Ruby's first few weeks at home here: kzbin.info/www/bejne/o3bVe3toi7qAb9Efeature=shared

Thank you for this video. Until a few years ago my ME was always very mild, to the point I often was confused and not 100% sure I had it. It's since become more mild-moderate, so I'm more sure that I have it, which my gp has always agreed with but because it was always so mild we never persued a specialist or formal diagnosis. I've never been at a point of need mobility aids, but recognise it potentially is in my future, specially as I'm now being tested for arthritis aswell & have pelvic issues & plantar fasciitis 😢 so this video has been useful for me, thank you 😊

I spent my 21st Birthday in Bruges in October 2005 we did the boat trip and a horse and cart tour then went up the tower which I will never do again I hated it was too hight but we had started drinking at like 11. o'clock clock that day and ended up in a super nice Irish Bar. thats was before I injured my neck. I do wanna go back at some point maybe next year for my 41st. glad u both had fun and that Izzy can do stuff while u are sleeping.

She is the cutest! Ive got a cavapoo called Minnie, she’s new aswell but she’s darker coloured

Now that I've had my chair for a bit, I had to come back to see which accessories you have. I think I need a different cup holder, as the one I have sits lower than it should. I have the higher back, which is GREAT, as it supports my back and shoulders better, so I'm not as fatigued by holding myself upright. If anyone's finding that you're getting shaken around, and tiring out your core, the higher back really helps. I have the arms on my chair up fairly high too, so I can rest my elbows and forearms on them easily, taking strain off my shoulders. Thanks for providing a list of the accessories you have - I don't have easy access to some of those specific items here in Canada, but at least I can look up what you've found useful, and aim for similar.

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How well do these handle hills?

kzbin.info/www/bejne/l4vCc598qs2Wmtk

I really wanted a robooter but you can’t get them on motability 😢 so this is a potential option

"What's wrong with you?" "I can't pull off a pixie cut. I've wanted to for ages but it wouldn't suit my face!"

Great vlog Pippa. I live in Bristol (on the outskirts) I am glad you had a relatively good time here, though the taxis do leave a lot to be desired. I am just getting started on my wheelchair journey, just got a basic self propelled wheelchair through the NHS, but looking at power add-ons to help out more, but finances are tight, so may be a little while yet. Having said that, I am so thrilled you showed the aquarium, I so want to visit it, as soon as I am able!! 😊

I've heard "ambulatory" pronounced differently in different countries - here in the U.S., it's am-byoo-luh-toh-ree.

I have POTS and EDS, but the main reason I use a wheelchair is because of an L5 incomplete spinal cord injury I sustained almost 9 years ago (no actual broken bones, but significant nerve pressure on my spinal cord that still frustratingly acts like it). I feel like I'm in an even rarer subset of ambulatory wheelies, because I can walk as far as I want on uneven surfaces without any issues (if uphill is involved, I might have to stop to catch my breath, but I'll be fine other than that), but on a smooth surface (like a sidewalk), my max is about 1/2 block before my left knee starts giving out on me (from the spinal nerve pressure). Thankfully my dr. has been great throughout this whole process, and I've found workarounds for some things, but there are times where my chair is my only way to get around even the house (usually I'm fine walking around the house without any aids).

For those unable to read these can you list them in a comment please?

I got ME after giving birth to my child. I spent the first three years at home, unable to do anything at all. In the end, I got a diagnosis and then a wheelchair. First a manual one, but it was immediatly clear that I can't manage a manual one, so I was placed on a wait list for a power wheelchair. The paperwork took forever to clear. So once I finally got mine, I cried. It was like I was finally free. I was finally able to be independent, go out and do stuff, but mainly save my energy so that I can do other things than just the very basic stuff. Today I can do a lot more, I'm no longer as fatigued as I used to, I'm not in as much pain as I used to and I don't feel trapped. It isn't just my physical health that improved with the wheelchair, my mental health got better. I also use a walker on the days I can walk or during the winter when I can't use the wheelchair due to the snow and ice. I have an Invacare Storm4, a huge all terrain beast. It can be adjusted in any way, including laying down like you would in a dentist chair. It does not have suspension though and it sucks big time. There's a newer model with suspension now. I'm going to try and have my occupational therapist to upgrade mine. I live in Sweden, so we get one chair from the government. Depending on where you live you can either get it for free or for a small annual fee (I unfortunately pay a fee). As for the financing: There are so many charities, foundations and organisations, both local and global that you can apply for mobility aid funds from. Just search for the ones that might work for you and apply. I don't know how it works in your country but in Sweden, a therapist can help you fill out an aplication. There's also so many accessories to get, so research what works for you and your chair. Power wheelchairs don't do well with cold weather, nor do they do well in snow. Keep that in mind and get winter weather options. There are raincoats for power wheelchairs that work wonders for rainy day weathers, and my favorite; the coldweather bag. It's basically a "sleeping" bag for wheelchairs designed to keep you dry and warm. Mine is lined with wool so it's warm even in really cold weather. Unfortuantely, my lungs hate cold air so I can't be outside at all during fall/winter or I cought my lungs out. I used to have a blanket but they don't really do much. A friend of mine made a cupholder for me in fabric. It can take a large water bottle, thermo mug, any bottle, cup or even snacks. I usually carry a plastic bag to cover the joystic with if it's just light rain. Since it's made of fabric it doesn't break when I hit a wall, or doorframe and it's really easy to push aside and clean. It does have it's perks knowing people who sew professionally.

I think you are great 👍 as a disable it can be same what hard. And in the Philippines it's impossible and even more so if you are non Philippineo. Craig Presnell ♿️

Cool vid and ship!

Thank you!

I had to come and watch, after enjoying your Málaga video! So wonderful about the accessible beach! Thanks for all the helpful information! 🙏❤

What a fun and informative episode! I loved it! ❤ I am very fortunate that I visited Spain ladt June, before my symptoms started. We flew into Málaga, but didn't stay there due to the expense of accommodation, but we had a fabulous time in many places that would be difficult for me to access now. At the moment I'm focusing on learning how to look after myself at home, but you've given me inspiration, that maybe I can travel again, with a bit of planning. Thanks so much!!! 🙏❤️

Please know that not all Christians believe you have to just believe in God harder or have a special prayer said over you in order to heal. I’m a Christian and severely chronically ill and no one in my church believes that. I wonder if Christians who believe that have ever read the book of Job or read 1 Corinthians 12:7-9 or John 9:2-3. God often allows us to suffer in order to bring us closer to Him and trust in Him alone for all things. The idea that the chronically ill and disabled just need to have more faith or that the illness or disability is always their fault due to sinfulness in their life is ridiculous. ❤ I highly recommend reading those Bible passages if you ever need comfort or guidance through the difficult days.😊 Great video as always!!!❤

Not that you need an excuse to return- but you could go for the purpose of visiting each accessible beach and doing a video guide. It would be so helpful to people planning their visit, and a fun excuse to play at beaches 😉

This was so helpful! First because I am absolutely living vicariously through you whilst bedridden - it is such a joy to see you out having adventures and being concious of energy expenditures. That hotel looks amazing and restful- and I loved your recharge sound, lol! Also because, if I can improve enough, I have a trip to Australia upcoming to visit my spouses aging parents and introduce them to their grandbaby. It looks like I won't get my power chair in time, so I will be looking into renting one upon arrival.

I really enjoyed this video!💚✨🥄 sending you spoons!🥄 I’m chronically ill and an ambulatory power chair user too!

Thank you for this informative and supportive video! ❤ I haven't got a diagnosis yet, a year after symptoms began, but now the symptoms are so chronic and disabling, that I'm pretty much housebound and struggling to care for myself. I have a walking stick, but that's it so far and it is a struggle to use when my arms are weak and painful. Definitely time to explore other mobility aids!

Thank you Pippa! I'm off to Greece tomorrow for the first time since a bad ME relapse a year ago. Although I know the area I'm travelling to well, it will be my first time with a power chair. Watching this vlog has really helped with the nerves!

I loooooove your travel vlogs!

I think this was one of your best videos so far. Very high production value and excellent and interesting content. It warmed my heart seeing you smile and having such a lovely time, you are well worth it. Can’t wait too see what you get up to next.

Not sure what's happening with your closed captions (might just be my device). Random sentences from later in video appearing alongside what you are saying in video at the time. Weird

Thank you Young lady! 👍👏💯

Thanks for sharing your trip with us!

If you did this trip again now, would you bring your Whill C2, or would you still rent?

I'm always watching for the local market, to buy some produce. Even for those without allergies, having access to a healthy snack like an apple or some good bread, can save you from buying a bag of snack food or sugary treats.

What do you think about freelancing or soloprenourship to skill up and rebuild confidence? Any thoughts? I also have M.E. (mild version of it)

You’re so much fun to listen to. No lie. I love your accent too

Thanks for watching everyone, really appreciate your kind words! If you've found yourself on this video recently, you might be interested in this updated video (2024) sharing my new power-chair, how I chose it, and how I accessed some funding: kzbin.info/www/bejne/kHnXfotofcmAa9Ufeature=shared And a tour of said powerchair here: kzbin.info/www/bejne/bHnReZSfjtKNqKMfeature=shared 🥰👩‍🦼‍➡

Wow! I wish I’d seen this video years ago! Thank you Pippa for sharing this, it should be essential viewing for those muddling through Long Covid like myself. I spent far too long stubbornly resisting adaptations and regret not taking the plunge much sooner. I was searching for mobility scooters vs powerchairs when I found this video (I bought a 2nd hand scooter and it was a game changer, and although it splits into parts and just fits into the car boot, those parts are so heavy!) so am contemplating switching to a foldable electric chair and ramp (there’s so much to think about, more so because I’m tall and heavy so that might well be a limiting factor). I thought the questions raised and your answers to them were fantastic, the ones around ambulatory use and perception by others have been things that bother me, it’s good to know it’s not just me who feels that way! Thank you again for making this - Subscribed! 🙌🙌🙌

Hello Pippa. My Name is Adri and I found you this week. I have purchased your audio book and am working thru your journal prompts. Your book is one of the most comprehensive books I have ever found. I was born with spastic and ataxic cerebral palsy. It’s from birth though due to the country I grew up in and various other reasons I wasn’t diagnosed until I was 16 years old. I always knew I was disabled but never viewed it as significant. Now I have Neuro Physical therapy and medication that addresses spasticity. I have a complex manual wheelchair and I have a carer to help me live in my own apartment by myself. I also utilize my service dog and we make a great team. I just wanted to honestly tell you I was one of the people who was skeptical about chronic fatigue and if it was a real medical issue. You in one weeks time with your videos have shown me how closed minded and rude I had been before. I think it was when you said it’s so much worse when a disabled person doesn’t understand what you’re going through. I don’t want be someone who gate keeps or excludes anyone. Thank you for your eloquent videos and genuine caring you demonstrate in your videos and through your book. I hope other disabled people re consider our views and bias toward ambulatory wheelchair users and people with chronic fatigue. I think the real reason I was close minded is because I didn’t take the time to validate my own frustrations with my disability. It really is important to support anyone with visible or invisible disability because at the end of the day we are all just trying our best. If anyone says you’re faking including doctors or friends and family, it’s more about that person than you. Keep going Pippa. I really enjoy your personality and clearly deeply thought out and planed videos. Congratulations on your book. It’s a joy to see what you’ve accomplished.

You did a great job on your audio book! You sound lovely. Bought it today. Congrats hun

Just bought your book hun! Listening to your narrating. I love your voice. So excited to enjoy this book and will share with my few close friends.

Congratulations on writing a book!